Canonical Allele Identifier: CA891841275
Gene: PTEN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.87961038_87961040delinsCTA , CM000672.2:g.87961038_87961040delinsCTA GRCh38
NC_000010.10:g.89720795_89720797delinsCTA , CM000672.1:g.89720795_89720797delinsCTA GRCh37
NC_000010.9:g.89710775_89710777delinsCTA NCBI36
NG_007466.2:g.102600_102602delinsCTA , LRG_311:g.102600_102602delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000700029.2:c.1039_1041delinsCTA ENSP00000514759.2:p.Leu347=
ENST00000710265.1:c.946_948delinsCTA ENSP00000518161.1:p.Leu316=
ENST00000472832.3:c.946_948delinsCTA ENSP00000483066.2:p.Leu316=
ENST00000688158.2:n.1681_1683delinsCTA
ENST00000688922.2:c.*776_*778delinsCTA ENSP00000508742.2:n.*776_*778delinsCTA
ENST00000700021.1:c.901_903delinsCTA ENSP00000514757.1:p.Leu301=
ENST00000700022.1:c.*285_*287delinsCTA ENSP00000514758.1:n.*285_*287delinsCTA
ENST00000700023.1:n.2104_2106delinsCTA
ENST00000700024.1:n.2338_2340delinsCTA
ENST00000700025.1:n.1715_1717delinsCTA
ENST00000700026.1:n.583_585delinsCTA
ENST00000706954.1:c.946_948delinsCTA ENSP00000516674.1:p.Leu316=
ENST00000706955.1:c.*981_*983delinsCTA ENSP00000516675.1:n.*981_*983delinsCTA
ENST00000686459.1:c.*532_*534delinsCTA ENSP00000508909.1:n.*532_*534delinsCTA
ENST00000688158.1:c.*1057_*1059delinsCTA ENSP00000509254.1:n.*1057_*1059delinsCTA
ENST00000688308.1:c.946_948delinsCTA ENSP00000508752.1:p.Leu316=
ENST00000688922.1:c.867_869delinsCTA
ENST00000693560.1:c.1465_1467delinsCTA ENSP00000509861.1:p.Leu489=
ENST00000371953.8:c.946_948delinsCTA MANE Select ENSP00000361021.3:p.Leu316=
ENST00000371953.7:c.946_948delinsCTA ENSP00000361021.3:p.Leu316=
ENST00000472832.2:c.373_375delinsCTA ENSP00000483066.1:p.Leu125=
NM_000314.5:c.946_948delinsCTA NP_000305.3:p.Leu316=
NM_000314.6:c.946_948delinsCTA NP_000305.3:p.Leu316=
NM_001304717.2:c.1465_1467delinsCTA NP_001291646.2:p.Leu489=
NM_001304718.1:c.355_357delinsCTA NP_001291647.1:p.Leu119=
XM_006717926.2:c.901_903delinsCTA XP_006717989.1:p.Leu301=
XM_011539981.1:c.946_948delinsCTA XP_011538283.1:p.Leu316=
XM_011539982.1:c.850_852delinsCTA XP_011538284.1:p.Leu284=
XR_945791.1:n.1516_1518delinsCTA
NM_000314.7:c.946_948delinsCTA NP_000305.3:p.Leu316=
NM_001304717.5:c.1465_1467delinsCTA NP_001291646.4:p.Leu489=
NM_001304718.2:c.355_357delinsCTA NP_001291647.1:p.Leu119=
NM_000314.8:c.946_948delinsCTA MANE Select NP_000305.3:p.Leu316=